ENST00000682153.1:c.*537G>C
|
ENSP00000507923.1:n.*537G>C
|
|
ENST00000682358.1:n.11513G>C
|
|
|
ENST00000683334.1:c.*7125G>C
|
ENSP00000507369.1:n.*7125G>C
|
|
ENST00000357162.7:c.11368G>C
MANE Select
|
ENSP00000349685.2:p.Glu3790Gln
|
|
ENST00000358544.7:c.11443G>C
MANE Plus Clinical
|
ENSP00000351346.2:p.Glu3815Gln
|
|
ENST00000357162.6:c.11368G>C
|
ENSP00000349685.2:p.Glu3790Gln
|
|
ENST00000358544.6:c.11443G>C
|
ENSP00000351346.2:p.Glu3815Gln
|
|
ENST00000493587.1:n.385G>C
|
|
|
NM_017890.4:c.11443G>C , LRG_351t1:c.11443G>C
|
NP_060360.3:p.Glu3815Gln
|
|
NM_152564.4:c.11368G>C , LRG_351t2:c.11368G>C
|
NP_689777.3:p.Glu3790Gln
|
|
XM_005250800.2:c.11443G>C
|
XP_005250857.1:p.Glu3815Gln
|
|
XM_005250801.3:c.11443G>C
|
XP_005250858.1:p.Glu3815Gln
|
|
XM_011516848.1:c.11440G>C
|
XP_011515150.1:p.Glu3814Gln
|
|
XM_011516849.1:c.11365G>C
|
XP_011515151.1:p.Glu3789Gln
|
|
XM_011516850.1:c.11065G>C
|
XP_011515152.1:p.Glu3689Gln
|
|
XM_011516851.1:c.8329G>C
|
XP_011515153.1:p.Glu2777Gln
|
|
XM_011516852.1:c.8329G>C
|
XP_011515154.1:p.Glu2777Gln
|
|
XM_011516854.1:c.7222G>C
|
XP_011515156.1:p.Glu2408Gln
|
|
XM_005250800.3:c.11443G>C
|
XP_005250857.1:p.Glu3815Gln
|
|
XM_005250801.5:c.11443G>C
|
XP_005250858.1:p.Glu3815Gln
|
|
XM_011516848.2:c.11440G>C
|
XP_011515150.1:p.Glu3814Gln
|
|
XM_011516849.2:c.11365G>C
|
XP_011515151.1:p.Glu3789Gln
|
|
XM_011516850.2:c.11065G>C
|
XP_011515152.1:p.Glu3689Gln
|
|
XM_011516851.2:c.8329G>C
|
XP_011515153.1:p.Glu2777Gln
|
|
XM_011516852.2:c.8329G>C
|
XP_011515154.1:p.Glu2777Gln
|
|
XM_011516854.2:c.7222G>C
|
XP_011515156.1:p.Glu2408Gln
|
|
XM_017013109.1:c.11248G>C
|
XP_016868598.1:p.Glu3750Gln
|
|
XM_017013111.1:c.8329G>C
|
XP_016868600.1:p.Glu2777Gln
|
|
XM_017013112.1:c.7000G>C
|
XP_016868601.1:p.Glu2334Gln
|
|
XM_024447074.1:c.10228G>C
|
XP_024302842.1:p.Glu3410Gln
|
|
NM_017890.5:c.11443G>C
MANE Plus Clinical
|
NP_060360.3:p.Glu3815Gln
|
|
NM_152564.5:c.11368G>C
MANE Select
|
NP_689777.3:p.Glu3790Gln
|
|